RBM14-RBM4 RBM14-RBM4 readthrough
Information
- Symbol
- RBM14-RBM4
- Type
- protein-coding
- Description
- RBM14-RBM4 readthrough
- Entrez Gene ID
- 100526737
- Genome
- hg19
- Position
- chr11:66,384,097-66,413,940
- Genome
- hg38
- Position
- chr11:66,616,626-66,646,469
- HGNC
- HGNC:38840 HGNC
- Ensembl
- ENSG00000248643 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 50 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | COAZ |
SYNONYM | PSP2 |
SYNONYM | RBM14 |
SYNONYM | SIP |
HGNC | HGNC:38840 HGNC |
Ensembl | ENSG00000248643 Ensembl |
AllianceGenome | HGNC:38840 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000500635.2 | hg38 | chr11 | 66,616,670 | 66,646,467 | 29,798 |
ENST00000412278.2 | hg38 | chr11 | 66,616,626 | 66,646,469 | 29,844 |
ENST00000412278.2 | hg19 | chr11 | 66,384,097 | 66,413,940 | 29,844 |
ENST00000500635.2 | hg19 | chr11 | 66,384,141 | 66,413,938 | 29,798 |
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